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Jost Schönberger

Showing results (1-10 of 7) with videos related to

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Medizinische Klinik (Munich, Germany : 1983)|March 18, 2008
[Monogenic heart disease]Jost Schönberger, Georg Ertl
Human Genetics|October 18, 2005
A novel locus for autosomal-dominant dilated cardiomyopathy maps to chromosome 7q22.3-31.1Jost Schönberger, Leif Kühler, Elisabete Martins, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society|July 27, 2011
Novel desmoplakin mutation: juvenile biventricular cardiomyopathy with left ventricular non-compaction and acantholytic palmoplantar keratodermaTatjana Williams, Wolfram Machann, Leif Kühler, et al.
Nature Genetics|March 1, 2005
Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing lossJost Schönberger, Libin Wang, Jordan T Shin, et al.
Circulation. Cardiovascular Genetics|October 27, 2015
Eya4 Induces Hypertrophy via Regulation of p27kip1Tatjana Williams, Moritz Hundertmark, Peter Nordbeck, et al.
The New England Journal of Medicine|February 23, 2007
Missense mutations in the BCS1L gene as a cause of the Björnstad syndromeJ Travis Hinson, Valeria R Fantin, Jost Schönberger, et al.
European Journal of Heart Failure|July 14, 2011
Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart FailureStephan Waldmüller, Jeanette Erdmann, Priska Binner, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Medizinische Klinik (Munich, Germany : 1983)|March 18, 2008
[Monogenic heart disease]Jost Schönberger, Georg Ertl
Human Genetics|October 18, 2005
A novel locus for autosomal-dominant dilated cardiomyopathy maps to chromosome 7q22.3-31.1Jost Schönberger, Leif Kühler, Elisabete Martins, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society|July 27, 2011
Novel desmoplakin mutation: juvenile biventricular cardiomyopathy with left ventricular non-compaction and acantholytic palmoplantar keratodermaTatjana Williams, Wolfram Machann, Leif Kühler, et al.
Nature Genetics|March 1, 2005
Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing lossJost Schönberger, Libin Wang, Jordan T Shin, et al.
Circulation. Cardiovascular Genetics|October 27, 2015
Eya4 Induces Hypertrophy via Regulation of p27kip1Tatjana Williams, Moritz Hundertmark, Peter Nordbeck, et al.
The New England Journal of Medicine|February 23, 2007
Missense mutations in the BCS1L gene as a cause of the Björnstad syndromeJ Travis Hinson, Valeria R Fantin, Jost Schönberger, et al.
European Journal of Heart Failure|July 14, 2011
Novel correlations between the genotype and the phenotype of hypertrophic and dilated cardiomyopathy: results from the German Competence Network Heart FailureStephan Waldmüller, Jeanette Erdmann, Priska Binner, et al.
Pageof 1